Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs10774037 0.882 0.040 12 2311360 intron variant G/A snv 0.77 2
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 2
rs10774035 0.925 0.040 12 2259508 intron variant C/A;T snv 1
rs4765913 1.000 0.040 12 2310730 intron variant A/T snv 0.82 1
rs4765914 0.925 0.040 12 2311211 intron variant T/C;G snv 1
rs7297582 0.925 0.040 12 2246640 intron variant C/T snv 0.29 1
rs10848642 1.000 0.040 12 2222406 non coding transcript exon variant A/G snv 0.37 1
rs10744560 0.882 0.040 12 2277933 intron variant C/G;T snv 1